JPS5895545A - Dispersant - Google Patents
DispersantInfo
- Publication number
- JPS5895545A JPS5895545A JP56193103A JP19310381A JPS5895545A JP S5895545 A JPS5895545 A JP S5895545A JP 56193103 A JP56193103 A JP 56193103A JP 19310381 A JP19310381 A JP 19310381A JP S5895545 A JPS5895545 A JP S5895545A
- Authority
- JP
- Japan
- Prior art keywords
- dispersant
- acid
- present
- dispersion
- unsatd
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、無機又は有機の微粉末を水中に分散するとき
に安定に分散させるために用いられる分散剤に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a dispersant used for stably dispersing inorganic or organic fine powder in water.
更に詳しくは、分散性が良好で且つ長時間保存しても微
粉末の沈降が少なくたとえ沈降しても凝固していわゆる
ハードケーキと呼ばれるものの生成が少な(、再分散性
が容易な、分散性を与える分散剤に関する。More specifically, it has good dispersibility, and there is little sedimentation of fine powder even when stored for a long time. This invention relates to a dispersant that provides
水難溶性または、水不溶性の無機又は有機の微粉末を、
水中に入れて分散させようとする場合、水と微粉末の比
重の差あるいは、微粉末の平均粒子径、粒度分布および
水に対する親和性、(1)
分散体の濃度、粘性などの諸因子が分散性に相互に関連
し、これら諸因子の適当なバランスが保持し得ないと微
粉末が沈喬したり、物によっては浮上したり、あるいは
、表面に浮いたままという様な状態になり分散しえない
状態になる。Slightly water-soluble or water-insoluble inorganic or organic fine powder,
When dispersing the powder in water, various factors such as the difference in specific gravity between water and the fine powder, the average particle size, particle size distribution, and affinity for water of the fine powder, (1) the concentration and viscosity of the dispersion, etc. Dispersibility is interrelated, and if an appropriate balance of these factors cannot be maintained, the fine powder may sink, float to the surface, or remain floating on the surface, resulting in poor dispersion. It becomes impossible to do so.
一般に微粉末の比重は、水より大きいので沈降するのが
殆どであるが、分散剤と呼ばれる化合物、例えば公知の
ポリオキシエチレーンオレイルエーテルなどの成る種の
界面活性剤を加えると、その作用で微粉末は、水中に安
定に懸濁し分散体となる。In general, the specific gravity of fine powder is greater than that of water, so most of the time it settles out, but when a compound called a dispersant, such as a surfactant such as the well-known polyoxyethylene oleyl ether, is added, its action is The fine powder is stably suspended in water to form a dispersion.
しかしこの分散体も本来、熱力学的には不安定なものな
ので、長時間放置すると、微粉末は必然的に沈降する。However, since this dispersion is inherently thermodynamically unstable, if left for a long time, the fine powder will inevitably settle.
一般に分散剤の分散性が良好なほど、分散体から沈降し
た微粉末は、細樹充填に近い沈降体となるので、硬く再
分散しにくい凝固体(即ちハードケーキ)をつくる、従
って分散体を作ったのち、それを使用する場合において
は、従来の分散剤で優れた分散性を有しているものは、
非常に有効なものであるが、分散体を長時間保存してか
ら使用する様な場合にこれらの分散剤を用いる(2)
と、ハードケーキが、生成され、再分散性が悪いという
問題が生じる。すなわち従来の分散剤は、微粉末の二次
粒子を一次粒子にほぐす作用と、はぐれた粒子が再び凝
集するのを防ぐ作用が強いが、沈降性及び沈降後のハー
ドケーキ生成防止の点で十分満足なものとはいえずこの
点改良が望まれている′。In general, the better the dispersibility of the dispersant, the finer the fine powder that settles out of the dispersion becomes a sediment that is closer to fine grain packing, creating a coagulate that is hard and difficult to redisperse (i.e., a hard cake). When using it after making it, conventional dispersants with excellent dispersibility are
Although these dispersants are very effective, if these dispersants are used when the dispersion is stored for a long time before use (2), a hard cake is formed and redispersibility is poor. arise. In other words, conventional dispersants have a strong effect of loosening fine powder secondary particles into primary particles and preventing separated particles from agglomerating again, but they are insufficient in terms of settling properties and preventing the formation of hard cakes after settling. This is not satisfactory and improvements are desired in this respect.
本発明者らは、微粉末に対し、優れた分散効果を有し、
沈降性および沈降後のハードケーキ生成を防止する分散
剤、特に沈降性が大きく、ハードケーキ生成が生じやす
い、比表面積が22000cd/g以下の如き平均粒子
径の大きい微粉末に対して従来の分散剤の欠点を改良し
た分散剤を見出すべく鋭意研究した結果、本発明の分散
剤を完成した。The present inventors have an excellent dispersion effect on fine powder,
A dispersing agent that prevents sedimentation and hard cake formation after sedimentation, especially conventional dispersion for fine powders with a large average particle size such as those with a specific surface area of 22,000 cd/g or less, which have a high sedimentation property and are prone to hard cake formation. As a result of intensive research to find a dispersant that improves the drawbacks of conventional dispersants, the dispersant of the present invention was completed.
即ち本発明は、α、β−不飽和カルボン酸とα。That is, the present invention provides α,β-unsaturated carboxylic acid and α.
β−不飽和アミド又はこれらと他のビニル系化合物を構
成成分とし、その10重量%水溶液の25℃における粘
度が800 cps以上20000 cps以下である
水溶性共重合体からなる分散剤に関す(3)
ものである。Concerning a dispersant consisting of a water-soluble copolymer containing β-unsaturated amide or these and other vinyl compounds, and whose 10% by weight aqueous solution has a viscosity of 800 cps or more and 20,000 cps or less at 25°C (3 ) It is a thing.
本発明の分散剤を用いることにより、分散体を長時間保
存しても沈降が少なく、しかも沈降物がハードケーキを
生成しない分散体を得ることがはじめて可能となった。By using the dispersant of the present invention, it has become possible for the first time to obtain a dispersion that exhibits little sedimentation even when the dispersion is stored for a long time, and in which the sediment does not form a hard cake.
本発明の分散剤になる共重合体を構成する成分であるα
、β−不飽和カルボン酸とはアクリル酸、メタクリル酸
、クロトン酸、マレイン酸、フマール酸、イタコン酸な
どであり、α、β−不飽和アミドとは、アクリルアミド
、メタクリルアミド等である。第3成分としてのビニル
系化合物としては、α、β−不飽和カルボン酸、α、β
−不飽和アミド以外の全てのビニル系化合物が含まれる
が、その代表例を挙げると、アクリル酸メチル、アクリ
ル酸エチル、アクリル酸プロピル、アクリル酸ブチル、
アクリル酸イソブチル、アクリル112エチルヘキシル
等のアクリル酸アルキルエステル類、メタクリル酸メチ
ル、メタクリル酸エチル、メタクリル酸プロピル、メタ
クリル酸ブチル、メタクリルjl12ヱチルヘキシル等
のメタクリル酸アルキ(4)
ルエステル類、アクリル酸2ヒドロキシエチル、メタア
クリル酸2ヒドロキシエチル等の如きアクリル酸又はメ
タアクリル酸のヒドロキシエステル類、酢酸ビニル、ス
テアリン酸ビニル等の如キビニルエステル類、アクリロ
ニトリル、メタクリロニトリル等の如き不飽和ニトリル
類、スチレン、α−メチルスチレン、α−クロルスチレ
ン、ビニルナフタリン、ビニルトルエンの如きビニル系
芳香族類、イタコン酸モノメチル、マレイン酸そツメチ
ル、マレイン酸ジブチル等の如き不飽和ジカルボン酸の
エステル類、グリシジルアクリレート、グリシジルメタ
クリレート、2エチルへキシルグリシジルエーテル等の
モノグリシジル誘導体、ジビニルベンゼン、ジビニルト
ルエン、フタル酸ジアリル、エチレングリコールジアク
リレート又はエチレングリコールジメタクリレートの如
き分子中に2個以上の不飽和結合を有する化合物類、ポ
リエチレングリコールモノメタクリレート、ポリプロピ
レングリコールモノメタクリレート、エチレングリコー
ルジグリシジルエーテル等のボリエ(5)
チレングリコール誘導体類、ビニルスルホン酸、アリル
スルホン酸、メタリルスルホン酸、スチレンスルホン酸
、2−アクリルアミドメチルプロパンスルホン酸等のス
ルホ基含有化合物類などが挙げられるが、これらの例に
限定されるものではなくミ他の一般的に既知の重合性を
有するビニル系化合物が広く使用出来る。しかしながら
水溶性共重合体を得るために、それらの使用量は必然的
に限定され、特に不飽和結合を2個以上有している化合
物の使用量は非常に限定された値となる。α, which is a component constituting the copolymer that becomes the dispersant of the present invention
, β-unsaturated carboxylic acids include acrylic acid, methacrylic acid, crotonic acid, maleic acid, fumaric acid, itaconic acid, etc., and α,β-unsaturated amides include acrylamide, methacrylamide, etc. Vinyl compounds as the third component include α, β-unsaturated carboxylic acids, α, β-unsaturated carboxylic acids,
- All vinyl compounds other than unsaturated amides are included; representative examples include methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate,
Acrylic acid alkyl esters such as isobutyl acrylate and acrylic 112 ethylhexyl, methacrylic acid alkyl esters such as methyl methacrylate, ethyl methacrylate, propyl methacrylate, butyl methacrylate, and methacrylic 112 ethylhexyl, acrylic acid dihydroxy Hydroxy esters of acrylic acid or methacrylic acid such as ethyl and dihydroxyethyl methacrylate; vinyl esters such as vinyl acetate and vinyl stearate; unsaturated nitrites such as acrylonitrile and methacrylonitrile; styrene; , vinyl aromatics such as α-methylstyrene, α-chlorostyrene, vinylnaphthalene, and vinyltoluene, esters of unsaturated dicarboxylic acids such as monomethyl itaconate, monomethyl maleate, dibutyl maleate, glycidyl acrylate, Monoglycidyl derivatives such as glycidyl methacrylate and 2-ethylhexyl glycidyl ether; compounds having two or more unsaturated bonds in the molecule such as divinylbenzene, divinyltoluene, diallyl phthalate, ethylene glycol diacrylate or ethylene glycol dimethacrylate; , polyethylene glycol monomethacrylate, polypropylene glycol monomethacrylate, ethylene glycol diglycidyl ether (5), tyrene glycol derivatives, vinyl sulfonic acid, allyl sulfonic acid, methallyl sulfonic acid, styrene sulfonic acid, 2-acrylamidomethylpropane sulfone Examples include sulfo group-containing compounds such as acids, but the present invention is not limited to these examples, and a wide variety of other generally known vinyl compounds having polymerizability can be used. However, in order to obtain a water-soluble copolymer, the amount of these compounds to be used is necessarily limited, and in particular, the amount of compounds having two or more unsaturated bonds is extremely limited.
本発明の分散剤の特長である分散性、沈降防止性および
ハードケーキ生成防止を達成するために好ましいものは
α、β−不飽和カルボン酸としてはアクリル酸又はメタ
クリル酸であり、α、β−不飽和アミドとしてはアクリ
ルアミドであり、第3成分のビニル系化合物としてはア
ルキル基の炭素数が1〜8であるアクリル酸アルキルエ
ステル又はメタクリル酸アルキルエステルであり、これ
らを組合せることによって本発明の特長をより良く発揮
させることができる。In order to achieve the dispersibility, anti-sedimentation properties, and prevention of hard cake formation, which are the features of the dispersant of the present invention, preferred α, β-unsaturated carboxylic acids are acrylic acid or methacrylic acid; The unsaturated amide is acrylamide, and the third component vinyl compound is an acrylic acid alkyl ester or a methacrylic acid alkyl ester in which the alkyl group has 1 to 8 carbon atoms.By combining these, the present invention can be achieved. You can make better use of your strengths.
(6)
α、β−不飽和カルボン酸の重合体もしくは共重合体及
びそれらの塩からなる分散剤についてはこれまでに種々
提案されてきているが、それらはいずれも本発明の目的
とする沈降性、ハードケーキ生成防止の改良については
殆どなし得ないものであり、いずれも分散性の改良のみ
を目的としているものにすぎない。(6) Various dispersants made of polymers or copolymers of α,β-unsaturated carboxylic acids and their salts have been proposed, but none of them have been proposed for the purpose of sedimentation, which is the object of the present invention. Almost no improvements can be made in terms of properties and prevention of hard cake formation, and all of these are merely aimed at improving dispersibility.
本発明の分散剤になる共重合体を構成する成分の組合せ
としては、
(1) α、β−不飽和カルボン酸/α、β−不飽和
アミド
(2) α、β−不飽和カルボン酸/α、β−不飽和
アミド/他のビニル系化合物
があるが、本発明の分散剤の目的とされる特長をより良
(発揮させるためには分散すべき微粉末によってことな
るが、(2)に示す成分からなる共重合体の方が+1)
に示される成分からなるものより優れていることが多い
。The combination of components constituting the copolymer that becomes the dispersant of the present invention is as follows: (1) α, β-unsaturated carboxylic acid/α, β-unsaturated amide (2) α, β-unsaturated carboxylic acid/ Although there are α,β-unsaturated amides/other vinyl compounds, (2) The copolymer consisting of the components shown in is +1)
It is often superior to those consisting of the ingredients shown in .
本発明の分散剤になる共重合体を構成する割合いについ
ては本発明の目的を達成するために構成(7)
成分全体を100重量部としてα、β−不飽和カルポン
酸20〜80重量部、α、β−不飽和アミド80〜20
重量部、ビニル系化合物0〜60重量部の割合が好まし
く、特に好ましい範囲は、α。The proportions constituting the copolymer that becomes the dispersant of the present invention are configured in order to achieve the object of the present invention (7) 20 to 80 parts by weight of α,β-unsaturated carboxylic acid, based on 100 parts by weight of the entire component , α, β-unsaturated amide 80-20
Parts by weight, the proportion of the vinyl compound is preferably 0 to 60 parts by weight, and a particularly preferable range is α.
β−不飽和カルボン酸20〜80重量部、α、β−不飽
和アミド10〜40重量部、ビニル系化合物lO〜40
重量である。ここにおいて、α、β−不飽和カルボン酸
が20重量部未満でα、β−不飽和アミドが80重量部
を越える場合は分散性が劣る様になり、α、β−不飽和
カルボン酸が80重量部を越え、α、β−不飽和アミド
が20重量部未満である場合は沈降性、ハードケーキ生
成防止が劣る様になる。20 to 80 parts by weight of β-unsaturated carboxylic acid, 10 to 40 parts by weight of α, β-unsaturated amide, 10 to 40 parts by weight of vinyl compound
It's weight. Here, if the α,β-unsaturated carboxylic acid is less than 20 parts by weight and the α,β-unsaturated amide exceeds 80 parts by weight, the dispersibility will be poor; If the amount of α,β-unsaturated amide exceeds 20 parts by weight, the sedimentation property and prevention of hard cake formation will be poor.
第3成分のビニル系化合物は本発明の特長をより発揮さ
せるために、必要に応じ加えられるものであるが、どの
ような場合においてもその量が60重量部を越える様に
なると分散性が劣る様になり好ましくない。The third component, a vinyl compound, is added as necessary in order to better exhibit the features of the present invention, but in any case, if the amount exceeds 60 parts by weight, the dispersibility will be poor. This is not desirable.
又、本発明の分散剤になる共重合体における、α、β−
不飽和カルボン酸から起因するカルホキ(8)
シル基は塩の形になっているものが水性分散体に適用が
容易な点からみて好ましい。塩の形の例としては、アル
カリ金属塩(リチウム、ナトリウム、カリウム塩など)
、アンモニウム塩、アミン塩(メチルアミン、ジェタノ
ールアミン塩など)を挙げることができる。なおこれら
のカルボキシキル基は未中和の部分を残しておいても差
しつかえがない。Moreover, in the copolymer used as the dispersant of the present invention, α, β-
The calhoki(8) sil group derived from an unsaturated carboxylic acid is preferably in the form of a salt from the viewpoint of ease of application to an aqueous dispersion. Examples of salt forms include alkali metal salts (lithium, sodium, potassium salts, etc.)
, ammonium salts, and amine salts (methylamine, jetanolamine salts, etc.). Note that there is no harm in leaving unneutralized portions of these carboxyl groups.
本発明の目的に対し、好適な分散剤を得るについては、
前述の共重合体構成成分及びその成分割合以外に、共重
合体分子量を特定のものにすることが必要で、特定の分
子量範囲のもののみが本発明の目的である特長を有する
のである。一般的に炭酸カルシウム、カオリン、クレー
、サチンホワイト等、各種微粉末顔料の分散剤として、
種々の重合体及び共重合体を用いることは知られており
、例えば、アクリルアミド/アクリル酸のアルカリ金属
塩共重合体(特公昭46−36883)、アクリル酸/
マレイン酸共重合物の塩(特開昭53−129200)
、高分子ポリカルボン酸または(9)
そのアルカリ金属塩(特開昭53−2557)、α、β
−不飽和酸/特定ビニル系化′合物の共重合体の塩(特
公昭5O−23850)等があるが、これらの重合体は
、全て、その分子量が100000以下を目標とし、い
わゆる低分子量側のものを用いて分散性を向上した従来
既知の分散剤としての使用を意図しており、これら低分
子量重合体の使用は本発明の目的とする沈降性およびハ
ードケーキ生成防止の場合、又特に微粉末の比表面積が
220GOcd/g以下の如き平均粒子の大きい微粉末
に適用させた場合において優れた分散効果は得られても
、分散後の放置による沈降が大きく、沈降ハードケーキ
を多く生成し、良好な分散体は得られない、又他の例と
して、ポリアクリルアミド及びアクリルアミド/アクリ
ル酸共重合体又は共重合体の塩で分子量が800万〜1
000万の如き、通常、高分子凝集剤として用いられる
様な高分子量を有する重合体を用いて、ゼオライトの安
定分散液を得る事も知られているが(特開昭55−84
533)、この様な分子量が凝集剤としく10)
て有効な高分子量の重合体の添加は、分散体の沈降及び
ハードケーキ生成の度合いは緩和出来ても本質的な分散
性に劣り、分散体の粘度が増大し、分散体の流動性が損
われるため分散体の取り扱い(作業性)及び他の配合原
料と混合された場合の実用品質上、支障が多く、一般的
に用いることは困難である。即ち本発明において上記に
詳述した通り、共重合体の構成成分が、α、β−不飽和
カルポン酸とα、β−不飽和アミドを必須成分とする二
元共重合体またはα、β−不飽和カルボン酸とα、β−
不飽和アミドおよび他のビニル系化合物との三元共重合
体で、且つ重合体の分子量を特定の範囲にすることによ
ってはじめて本発明の目的を達成する分散剤が得られた
のである。しかしながらこれらの共重合体の分子量につ
いていえば該共重合体の正確な分子量の絶対値を得るこ
とは、測定技術上、種々難点があるため、本発明分散剤
については、分子量と関連性の大きい重合体の溶液粘度
において特定するものであり、B型精度針で25℃にお
いてローター回転数5 Q rpmで測定(11)
した10重量%水水溶液25℃における粘度範囲で規定
するものであり、本発明に係わる共重合体におl、N”
(は800 cps以上20000 cps以下であり
、好ましくは10000 cps以下である。即ち80
0 cps以下では分散性は優れていても分散後の沈降
が大きく、ハードケーキも容易に生成する。又、200
00 cpsを越えた場合分散性が劣り、分散体の粘度
が増大し、流動性に劣り作業性が著しく劣化する。この
水溶液粘度(800〜20000 cps )と平均分
子量との関連は、本発明に係わる共重合体について、明
確に表すことは出来ないが、凡その平均分子量としては
15万〜85万と推定される。To obtain a dispersant suitable for the purpose of the present invention,
In addition to the above-mentioned copolymer components and their component proportions, it is necessary to specify the molecular weight of the copolymer, and only those within a specific molecular weight range have the features that are the object of the present invention. Generally used as a dispersant for various fine powder pigments such as calcium carbonate, kaolin, clay, and satin white.
It is known to use various polymers and copolymers, such as acrylamide/alkali metal salt copolymer of acrylic acid (Japanese Patent Publication No. 46-36883), acrylic acid/
Salt of maleic acid copolymer (JP-A-53-129200)
, high molecular weight polycarboxylic acid or (9) its alkali metal salt (JP-A-53-2557), α, β
- There are salts of copolymers of unsaturated acids/specific vinyl compounds (Japanese Patent Publication No. 5O-23850), but all of these polymers aim to have a molecular weight of 100,000 or less, so-called low molecular weight These low molecular weight polymers are intended to be used as conventionally known dispersants with improved dispersibility, and the use of these low molecular weight polymers is useful for the purpose of the present invention in preventing sedimentation and hard cake formation. In particular, when applied to fine powder with a large average particle size, such as a fine powder with a specific surface area of 220 GOcd/g or less, even if an excellent dispersion effect is obtained, there is a large amount of sedimentation due to standing after dispersion, and a large amount of sedimentation hard cake is generated. Another example is polyacrylamide and acrylamide/acrylic acid copolymers or salts of copolymers with a molecular weight of 8 million to 1.
It is also known that a stable dispersion of zeolite can be obtained by using a polymer having a high molecular weight such as 0 million, which is usually used as a polymer flocculant (Japanese Patent Laid-Open No. 55-84).
533), the addition of polymers with such high molecular weights, which are effective as flocculants10), can reduce the degree of sedimentation and hard cake formation of the dispersion, but the essential dispersibility is poor and the dispersion This increases the viscosity of the dispersion and impairs the fluidity of the dispersion, causing many problems in terms of handling (workability) of the dispersion and practical quality when mixed with other blended raw materials, making it difficult to use in general. It is. That is, as detailed above in the present invention, the constituent components of the copolymer are a binary copolymer containing α,β-unsaturated carboxylic acid and α,β-unsaturated amide as essential components, or α,β- Unsaturated carboxylic acids and α, β-
A dispersant that achieves the objects of the present invention was obtained by using a terpolymer of unsaturated amide and other vinyl compounds and by controlling the molecular weight of the polymer within a specific range. However, when it comes to the molecular weight of these copolymers, there are various difficulties in measuring technology in obtaining accurate absolute values of the molecular weight of the copolymer. It is specified by the solution viscosity of the polymer, and is defined by the viscosity range of a 10% aqueous solution at 25°C, measured with a B-type precision needle at 25°C and a rotor rotation speed of 5 Q rpm (11). l, N” in the copolymer according to the invention
(is 800 cps or more and 20,000 cps or less, preferably 10,000 cps or less. That is, 80
At 0 cps or less, even if the dispersibility is excellent, the sedimentation after dispersion is large and hard cakes are easily formed. Also, 200
If it exceeds 0.00 cps, the dispersibility will be poor, the viscosity of the dispersion will increase, the fluidity will be poor, and the workability will be significantly deteriorated. Although the relationship between the aqueous solution viscosity (800 to 20,000 cps) and the average molecular weight cannot be clearly expressed for the copolymer according to the present invention, the average molecular weight is estimated to be approximately 150,000 to 850,000. .
以上本発明の目的を達成する分散剤及びその構成要件を
詳細に述べたが、本発明の分散剤は公知重合体の分散剤
では明らかにされていない構造を有し、又その目的にお
いても従来の分散剤では達しえなかった分散性、沈降防
止性、ハードケーキ生成防止の特性のいずれにおいても
優れた効果が得られ、従来の分散剤では見られない顕著
な利点を(12)
発揮するものである。Although the dispersant and its constituent requirements for achieving the object of the present invention have been described in detail above, the dispersant of the present invention has a structure that has not been clarified in known polymer dispersants, and also has a structure that has not been clarified in conventional polymer dispersants for that purpose. It has excellent effects in terms of dispersibility, anti-settling properties, and prevention of hard cake formation that could not be achieved with conventional dispersants (12). It is.
本発明の分散剤の使用にあたっては、分散剤を分散体(
微粉末+水)に対し0.005〜3重量%の割合で使用
すればよく、好ましくは、0.01〜1.5重量%の割
合で添加するのが望ましい。When using the dispersant of the present invention, the dispersant must be used as a dispersant (
It may be used in an amount of 0.005 to 3% by weight, preferably 0.01 to 1.5% by weight, based on the fine powder+water.
本発明の分散剤は、無機及び有機のいずれの微粉末に対
しても有効であり、例えば無機粉末としては、酸化チタ
ン、炭酸カルシウム、クレー、酸化亜鉛、酸化鉄、サチ
ンホワイト、硫酸バリウム、ホワイトカーボン、紺青、
群青、カーボンブラック、水酸化アルミニウム等、有機
粉末としては、不溶性アゾ顔料、アゾ系分散染料、フタ
ロシアニン系顔料、スレン染料、アントラキノン系分散
染料、レーキ顔料、石炭粉末などである。The dispersant of the present invention is effective for both inorganic and organic fine powders. Examples of inorganic powders include titanium oxide, calcium carbonate, clay, zinc oxide, iron oxide, satin white, barium sulfate, white carbon, dark blue,
Examples of organic powders such as ultramarine, carbon black, and aluminum hydroxide include insoluble azo pigments, azo disperse dyes, phthalocyanine pigments, threne dyes, anthraquinone disperse dyes, lake pigments, and coal powder.
また本発明の分散剤は使用に当って微粉末の粒子径によ
って何等制限を受けるものでなく、どの様な粒子径のも
のに対しても良好な効果を示すが、比表面積が2200
0d/g以下の平均粒子径が比較的大きい微粉末は沈降
性が大きいためその様な微粉末に用いることにより特に
本発明の効果を(13)
顕著に引き出すことができる0分散体における微粉末濃
度は分散体が生成されるいずれの濃度でもよく、一般に
0.5〜80重量%が殆どであり、その様な濃度におい
て本発明の分散剤は何等支障なく使用できる。In addition, the dispersant of the present invention is not limited in any way by the particle size of the fine powder in use, and shows good effects on particles of any size.
Since fine powders with a relatively large average particle size of 0 d/g or less have a high sedimentation property, by using such fine powders, the effects of the present invention can be particularly brought out (13). The concentration may be any concentration at which a dispersion is produced, generally from 0.5 to 80% by weight, and the dispersant of the present invention can be used at such concentrations without any problems.
本発明の分散剤の使用に際して、アトライター、サンド
ミル、三本ロール、ボールミル、ホモジナイザーなど一
般に既知の分散機乃至粉砕機を用いてよく、又本発明の
分散剤は、単独使用の他、他の一般的な水系分散剤、た
とへばアニオン性、及びノニオン性界面活性剤、ポリア
クリル酸ナトリウム、オレフィン/マレイン酸ナトリウ
ム共重合体等などの重合体系分散剤、及び縮合リン酸塩
等を併用することは何等差仕えない、又、本発明の分散
剤は、前記した無機及び有機系微粉末が使用されるいず
れの分野に於ても適用されるが、例えば、紙加工、繊維
加工、建材加工、セラミック、顔料製造、塗料などの広
範囲の分野に適用出来る。When using the dispersant of the present invention, generally known dispersing machines or pulverizers such as an attritor, sand mill, three-roll mill, ball mill, or homogenizer may be used. General aqueous dispersants, anionic and nonionic surfactants, polymeric dispersants such as sodium polyacrylate, olefin/sodium maleate copolymers, etc., and condensed phosphates cannot be used together. Moreover, the dispersant of the present invention can be applied to any field where the above-mentioned inorganic and organic fine powders are used, such as paper processing, textile processing, building material processing, ceramic processing, etc. It can be applied to a wide range of fields such as , pigment production, and paints.
以下、本発明を実施例及び比較例により、具体的に示す
。Hereinafter, the present invention will be specifically illustrated with reference to Examples and Comparative Examples.
(14)
実施例及び比較例
微粉末として、重質炭酸カルシウム(比表面積3500
cd/g、平均粒子径6.35μ)を用いて各種分散剤
につき、下記の試験を行い別表に示す結果を得た。(14) Examples and Comparative Examples As fine powder, heavy calcium carbonate (specific surface area 3500
cd/g, average particle diameter 6.35μ), the following tests were conducted on various dispersants, and the results shown in the attached table were obtained.
所定量の水に分散剤を加え、ラボディスパーで攪拌しな
がら(2000rpn+)、上記粉末を徐々に加え、全
量を添加してから、更に10分間攪拌しスラリー濃度7
5%の炭酸カルシウムスラリーを得た。(分散剤は純分
で炭酸カルシウムに対し0゜1%を使用した)
得られたスラリーについて、配合直後の分散性、及びそ
のスラリーを2日間、常温放置した場合の沈降性とハー
ドケーキ生成についての評価試験を行い、別表に示す結
果を得た。結果に示す通り、本発明の分散剤を使用した
場合は、分散性、沈降性、ハードケーキ生成防止のいず
れの評価に於ても良好な結果を示し極めて良好な、分散
剤と言える。本発明範囲外の分散剤を用いた場合は、評
価項目の内、少なくともいずれかの項目に不満足な(1
5)
結果を示し、本発明の目的を果さない。Add the dispersant to a predetermined amount of water, and while stirring with a lab body spar (2000 rpm+), gradually add the above powder. After adding the entire amount, stir for another 10 minutes until the slurry concentration is 7.
A 5% calcium carbonate slurry was obtained. (The pure content of the dispersant was 0.1% based on calcium carbonate.) About the obtained slurry, the dispersibility immediately after blending, and the sedimentation and hard cake formation when the slurry was left at room temperature for 2 days. An evaluation test was conducted and the results shown in the attached table were obtained. As shown in the results, when the dispersant of the present invention was used, it showed good results in all evaluations of dispersibility, sedimentation, and prevention of hard cake formation, and can be said to be an extremely good dispersant. If a dispersant outside the scope of the present invention is used, it may be unsatisfactory in at least one of the evaluation items (1.
5) Shows results and does not serve the purpose of the present invention.
尚、各試験項目の評価判定法は次の通りである。The evaluation method for each test item is as follows.
〔分散性〕 ニスラリ−配合直後の粘度を測定。[Dispersibility] Measure the viscosity immediately after blending Nislary.
(25℃、60 rpm、90秒後の値を読む)
〔沈降性〕 :得られたスラリーを無攪拌下に常温
・で2日間放置し、粒子が沈降せずに
分散しているかどうかにより目視評
価した。(25°C, 60 rpm, read the value after 90 seconds) [Settling property]: The obtained slurry was kept at room temperature without stirring.
・The sample was left for 2 days and visually evaluated to determine whether the particles were dispersed without settling.
○・・・沈降していない。○...No sedimentation.
Δ・・・僅かに沈降している。Δ... Slight sedimentation.
×・・・沈降物が非常に多い。×: There is a large amount of sediment.
〔ハードケーキ生成〕 :沈降性と同様2日間放置後の
スラリーについて次
の様に評価した。[Hard cake formation]: Similar to the sedimentation property, the slurry after being left for 2 days was evaluated as follows.
○・・・ハードケーキの生成ないもの。○: No hard cake formation.
△・・・ケーキの生成はあるが再分散容易なもの。△: Cake was formed, but redispersion was easy.
×・・・明らかにハードなケーキが生成し再分散が難し
いもの。×: Obviously a hard cake is formed and redispersion is difficult.
(16)(16)
Claims (1)
これらと他のビニル系化合物を構成成分とし、その10
重量%水溶液の25℃における粘度が800 cps以
上20000 cps以下である水溶性共重合体からな
る分散剤。α, β-unsaturated carboxylic acid, α, β-unsaturated amide, or these and other vinyl compounds as constituent components, and 10
A dispersant comprising a water-soluble copolymer having a viscosity of 800 cps or more and 20,000 cps or less at 25° C. in a wt% aqueous solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56193103A JPS5895545A (en) | 1981-11-30 | 1981-11-30 | Dispersant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56193103A JPS5895545A (en) | 1981-11-30 | 1981-11-30 | Dispersant |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5895545A true JPS5895545A (en) | 1983-06-07 |
JPS6321525B2 JPS6321525B2 (en) | 1988-05-07 |
Family
ID=16302283
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56193103A Granted JPS5895545A (en) | 1981-11-30 | 1981-11-30 | Dispersant |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5895545A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62241549A (en) * | 1986-04-14 | 1987-10-22 | Sanko Kaihatsu Kagaku Kenkyusho:Kk | Method for dispersing polyvalent metallic salt of organic acid |
US5021526A (en) * | 1988-07-05 | 1991-06-04 | The Standard Oil Company | Anionic polymeric stabilizers for oil-in-water emulsions |
JPH03188103A (en) * | 1983-12-26 | 1991-08-16 | Nippon Zeon Co Ltd | Dispersant for dispersing fine particulate material in medium |
US5213893A (en) * | 1990-09-14 | 1993-05-25 | Nippon Shokubai Co., Ltd. | Waterproofing agent for cable |
JPH06207134A (en) * | 1992-11-06 | 1994-07-26 | Nippon Carbide Ind Co Inc | Water-based coating composition |
JP2010526901A (en) * | 2007-05-11 | 2010-08-05 | オムヤ・デイベロツプメント・アー・ゲー | Method for grinding minerals and binders in aqueous media using an inverse emulsion of a polymer of acrylamide containing acrylic monomers |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06190660A (en) * | 1992-12-28 | 1994-07-12 | Mitsubishi Motors Corp | Carry-in device for body outfitting parts |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5137539A (en) * | 1974-07-29 | 1976-03-29 | Redactron Corp | Tanitsuyosopurinta |
-
1981
- 1981-11-30 JP JP56193103A patent/JPS5895545A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5137539A (en) * | 1974-07-29 | 1976-03-29 | Redactron Corp | Tanitsuyosopurinta |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03188103A (en) * | 1983-12-26 | 1991-08-16 | Nippon Zeon Co Ltd | Dispersant for dispersing fine particulate material in medium |
JPH0567333B2 (en) * | 1983-12-26 | 1993-09-24 | Nippon Zeon Co | |
JPS62241549A (en) * | 1986-04-14 | 1987-10-22 | Sanko Kaihatsu Kagaku Kenkyusho:Kk | Method for dispersing polyvalent metallic salt of organic acid |
US5021526A (en) * | 1988-07-05 | 1991-06-04 | The Standard Oil Company | Anionic polymeric stabilizers for oil-in-water emulsions |
US5213893A (en) * | 1990-09-14 | 1993-05-25 | Nippon Shokubai Co., Ltd. | Waterproofing agent for cable |
JPH06207134A (en) * | 1992-11-06 | 1994-07-26 | Nippon Carbide Ind Co Inc | Water-based coating composition |
JP2010526901A (en) * | 2007-05-11 | 2010-08-05 | オムヤ・デイベロツプメント・アー・ゲー | Method for grinding minerals and binders in aqueous media using an inverse emulsion of a polymer of acrylamide containing acrylic monomers |
Also Published As
Publication number | Publication date |
---|---|
JPS6321525B2 (en) | 1988-05-07 |
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